EP1522575A1 - Compositions détergentes - Google Patents

Compositions détergentes Download PDF

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Publication number
EP1522575A1
EP1522575A1 EP04077426A EP04077426A EP1522575A1 EP 1522575 A1 EP1522575 A1 EP 1522575A1 EP 04077426 A EP04077426 A EP 04077426A EP 04077426 A EP04077426 A EP 04077426A EP 1522575 A1 EP1522575 A1 EP 1522575A1
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EP
European Patent Office
Prior art keywords
phase
soap
tablet
composition
region
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP04077426A
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German (de)
English (en)
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EP1522575B1 (fr
Inventor
Arjen Jacco Hoekstra
Duncan Howard Wright
Lammert Nauta
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Unilever PLC
Unilever NV
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Unilever PLC
Unilever NV
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Priority to EP20040077426 priority Critical patent/EP1522575B1/fr
Publication of EP1522575A1 publication Critical patent/EP1522575A1/fr
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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0073Tablets
    • C11D17/0078Multilayered tablets

Definitions

  • This invention relates to cleaning compositions in the form of tablets for example, for use in fabric washing or machine dishwashing.
  • Detergent compositions in tablet form have advantages over powdered products in that they do not require measuring and are thus easier to handle and dispense into the wash-load.
  • Tablets of a cleaning composition are generally made by compressing or compacting a quantity of the composition in particulate form.
  • WO 01/42416 describes the production of multi-phase moulded bodies comprising a combination of core moulded bodies and a particulate premix.
  • WO 00/61717 describes a detergent tablet which is characterised in that at least part of its outer surface is semi-solid.
  • WO 00/04129 describes a multi-phase detergent tablet comprising a first phase in the form of a shaped body having at least one mould therein and a second phase in the form of a particulate solid compressed within said mould.
  • a cleaning tablet which has a plurality of discrete regions with differing compositions, characterised in that at least one first region of the tablet is a soap rich region and at least one second region of the tablet is a solid region of compacted particulate material.
  • the invention also relates to a method for producing a cleaning tablet comprising a soap rich phase, wherein the production of the soap rich phase comprises the compression of a particulate composition comprising at least 50 %wt of detergent particles, wherein said detergent particles comprise at least 10 %wt, preferably at least 25% wt, more preferably at least 50% wt, of soap.
  • tablets of the invention are of cylindrical shape (e.g. round, rectangular or square) wherein the two main surfaces (upper side and bottom side) are substantially flat.
  • tablets of the invention are multiphase tablets wherein the soap rich phase is present and additionally one phase of compacted particulates is present. Suitably there may be additional phases to the compressed phase and the soap rich phase.
  • the cleaning tablet further comprises at least one smooth phase. Most advantageous is the location of the soap rich phase as a barrier between the compressed phase and the smooth phase. Surprisingly it has been found that the soap rich layer significantly reduced the bleeding of ingredients from the smooth phase into the compressed phase, without unduly affecting the cleaning properties and dissolution properties of the cleaning tablet.
  • the regions of a multi-phase tablet are preferably separate layers within a cleaning tablet.
  • a discrete region of a tablet could also have other forms for example one or more core(s) or insert(s).
  • the first region is a soap rich layer and the second region is a layer of compacted particulate material.
  • the tablet is a multi-phase tablet comprising the soap rich phase of the invention
  • the soap rich phase is present as a distinctive region preferably having a weight of from 2 to 40 grammes, more preferred from 3 to 20 grammes, most preferred from 4 to 10 grammes.
  • the other phases each have a weight of 2 to 40 grammes.
  • the total weight of the cleaning tablet according to the invention is from 10 to 100 grammes, more preferred from 15 to 60 grammes, most preffered from 15 to 50 grammes.
  • soap rich phase refers to a separate part of the tablet, e.g. a region, such as a layer, wherein the level of soap is at least 10% wt, more preferably at least 15% wt, still more preferably at least 20% wt, yet more preferably at least 25% wt.
  • Typical soap levels in the soap rich phase are from 15% to 50% by weight, more preferably from 25% to 40% by weight.
  • the soap level is at least 50% wt and can even be very high say more than 80wt% or even more than 90 %wt up to 100 %wt based on the weight of the soap rich phase.
  • soap rich layer may also be present in the soap rich layer, although preferably the soap rich layer is substantially free of non-soap surfactants, bleach ingredients and builder materials.
  • a highly soluble material such as sugars, urea, alkali metal salts such as sodium chloride etc.
  • highly soluble materials will have a solubility of at least 100 grammes per litre water of 20 C, more preferred at least 250 grammes.
  • the level of these highly soluble materials in the soap rich phase is less than 50%wt, for example from 5 to 45 %wt, advantageously from 10 to 40 %wt.
  • the soap rich region of the tablet may be prepared by any suitable method for example the spraying, applying or brushing of a soap rich formulation, if appropriate followed by hardening e.g. by cooling.
  • the soap rich layer is obtained from the compression of soap rich particles.
  • Such detergent particles preferably comprise at least 10 %wt, more preferably at least 50%wt (based on the particles) of soap surfactants.
  • Suitable detergent particles may for example be granules or other particles having high soap levels, for example soap noodles, marumes or granulates with high soap levels.
  • the level of soap surfactants in the soap rich particles is more than 50 %wt, more preferred more than 70 %wt, especially preferred from 75 %wt to 100 %wt.
  • the level of soap rich particles in the soap rich phase is at least 60 wt%, more preferred from 80 to 100 wt%.
  • surfactants for example anionic, nonionic or cationic surfactants may equally be present in the soap rich phase for example at a level of 0.1 to 10 %wt based on the weight of the soap rich part. However normally the first soap rich phase will be substantially free from non-soap surfactants.
  • the soap rich region may comprise other materials for example soluble materials such as electrolyte materials, meltable organic materials and sugars, at a level of 2 to 70 %wt based on the weight of the smooth part, more preferred from 3 to 50 %wt, most preferred 5 to 40 wt%.
  • soluble materials such as electrolyte materials, meltable organic materials and sugars
  • water-soluble materials such as the sodium and potassium citrates, sodium chloride, acetates and carbonates, urea and sugar.
  • the water solubility at 20 C of these materials is preferably at least 10 grammes per 100 ml of water, more preferred more than 15 grammes, most preferably more than 20 grammes.
  • soap rich phase is a soap rich continuous matrix having dispersed therein particles of the water soluble material.
  • the cleaning tablet comprises in addition to the soap rich phase and the compressed phase a smooth phase.
  • smooth phase refers to compositions which are on the one hand solid enough to retain their shape at ambient temperature and on the other hand smooth in appearance. Smooth textures are generally of low or no porosity and have -at normal viewing distance- the appearance of a continuous phase for example as opposed to porous and particulate appearance of a compacted particulate material.
  • the smooth region of the tablet may also contain diluent materials for example polyethyleneglycol, dipropyleneglycol, isopropanol or (mono-)propyleneglycol.
  • diluent materials for example polyethyleneglycol, dipropyleneglycol, isopropanol or (mono-)propyleneglycol.
  • the level of these diluents is from 0 to 40 %wt, more preferred 1 to 20, most preferred from 4 to 15 %wt based on the weight of the smooth phase.
  • the smooth phase comprises no or only low levels of water.
  • the level of water is less than 20 wt % based on the weight of the smooth phase, more preferred less than 15 wt%, most preferred from 5 to 12 wt%.
  • the smooth phases are substantially free from water, which means that apart from low levels of moisture (e.g. for neutralisation or as crystal water) no additional added water is present.
  • the smooth phase is transparent or translucent.
  • this means that the composition has an optical transmissivity of at least 10%, most preferably 20%, still more preferably 30%, through a path length of 0.5 cm at 25° C.
  • These measurements may be obtained using a Perkin Elmer UV/VIS Spectrometer Lambda 12 or a Brinkman PC801 Colorimeter at a wavelength of 520nm, using water as the 100% standard.
  • compositions according to the invention does not preclude the composition being coloured, e.g. by addition of a dye, provided that it does not detract substantially from clarity.
  • the smooth phase comprises from 30-100 %wt of non-soap surfactants, more preferred 40 to 90 %wt (based on the total weight of said smooth phase), more preferred from 50 to 80 %wt. It has been found that the combination of a separate smooth first region and these high non-soap surfactant levels provide very good dispersing and cleaning properties to the tablet.
  • the total weight of surfactants in the smooth phase is from 2 to 20 grammes, more preferred from 3 to 10 grammes.
  • the tablet may be a multi-phase tablet wherein the phases other than the smooth phase as described above comprise no or only low levels of non-soap surfactants.
  • the level of non-soap surfactants in the solid phases is less than 10 %wt (based on the total weight of said phases), more preferred from 0 to 9 %wt, most preferred from 1 to 8 %wt.
  • the cleaning tablets comprise a first soap rich region (as described above) in combination with a second region of the tablet which is a solid region, for example prepared by compression of a particulate composition.
  • cleaning tablets of the invention also comprise a third smooth region (as described above)
  • the second region may comprise surfactant materials
  • this region preferably comprises ingredients of the tablet other than surfactants.
  • these ingredients are for example builders, bleach system, enzymes etc.
  • the builders in the tablet are predominantly present in the second region.
  • the bleach system is predominantly present in the second region.
  • the enzymes are predominantly present in the second region.
  • the term "predominantly present” refers to a situation wherein at least 90 %wt of an ingredient is present in the second region, more preferred more than 98 %wt, most preferred substantially 100 %wt.
  • the cleaning tablets comprise a first soap rich region (as described above) in combination with a third smooth region.
  • a third smooth region advantageously comprises 50-100 %wt of non-soap surfactants for examples 60 to 90 %wt in combination with optional ingredients such as to 0 to 50 wt% soluble materials (as described above) 0 to 40 wt% diluent materials (as described above) and 0 to 20 wt% (as described above) of water.
  • the non-soap surfactants in said third smooth phase may for example be anionic, nonionic or cationic non-soap surfactants or mixtures thereof. Relatively low levels of soap may also be present, for example up to 10 %wt based on said third smooth phase.
  • the tablet has been given with reference to a tablet constituted by two or three regions. It will however be understood that each of the regions may be composed of a limited number of discrete regions.
  • the first soap rich region may be a single discrete part of the tablet but may also be a limited number (say 1-5) discrete soap rich parts.
  • each of these soap rich parts are at least 2 grammes, also preferably each of these soap rich parts may be substantially of the same composition or of different composition. If reference is made to the composition or weight of the first region it is understood that this concerns the total weight and composition of these soap rich parts.
  • the solid second region may be composed of a limited number (say 1-5) of solid parts e.g. separate layers in the tablet.
  • each of these parts has a weight of at least 10 grammes, also preferably each of the solid parts is substantially of the same composition. If reference is made to the composition or weight of the second region it is understood that this concerns the total weight and composition of these solid parts.
  • An especially preferred embodement of the invention relates to a multi-phase cleaning tablet comprising a soap rich first phase (as described above) in combination with a non-soap surfactant rich second smooth phase (as described above) and a solid region, for example as prepared by compression of a particulate compostion.
  • each of the regions in this preferred embodiment has a weight of 2 to 50 grammes.
  • the soap rich phase is from 2 to 20 grammes for example 3 to 15 grammes.
  • the non-soap surfactant rich phase is from 2 t 20 grammes, for example 3 to 15 grammes.
  • the solid phase is from 5 to 50 grammes, for example 10 to 40 grammes.
  • the regions are present as layers in the cleaning tablet.
  • Cleaning tablets according to the invention are preferably manufactured by a process involving the application of pressure to a particulate mixture.
  • the preparation of the soap rich phase may involve the dosing of a particulate mixure comprising soap rich particles optionally in combination with other materials as described above, followed by the exertion of pressure, preferably above the yield stress of the soap rich particles. It has been found that the exertion of pressure to a particulate mixture comprising significant levels of soap rich particles leads to a certain flow behaviour of the mixture leading to the formation of a continuous, soap rich phase.
  • Detergent particles for use in the preparation of the soap rich phase preferably have a relatively high soap level of at least 10% wt, more preferred more than 50 %wt, yet more preferred more than 55 %wt, most preferred from 60 to 90 or even 100 %wt.
  • a multi-phase tablet comprising a soap rich phase may advantageously be made by a process, comprising the steps of:
  • step (a) takes place before step (b).
  • the first particulate composition is such that upon compression a solid phase of compressed particulate material is formed.
  • the first particulate composition is pre-compressed at a force of 0.1 to 20 kN/cm 2 between steps (a) and (b). In another preferred embodiment, the particulate composition is flattened between steps (a) and (b).
  • the (co-) compression of the combination of the soap rich and the solid region(s) takes place at a force of from 0.05 to 20 kN/cm 2 .
  • the co-compression in step (c) can advantageously be at a force of 0.1- 10 kN/cm 2 , more preferred 0.5 to 5 kN/cm 2 .
  • the co-compression preferably takes place at a force of 1- 100 kN/cm 2 ., more preferred 2-50 kN/cm 2 ., most preferred 2-10 kN/cm 2 .
  • the tablet of the invention comprises a soap-rich phase as described above this phase may also be manufactured seperately by compression of a particulate soap rich material e.g. at the compation forces as indicated above.
  • the soap rich phase may be prepared by other methods for example the spraying of a soap rich composition for example onto the (pre) compressed compacted tablet phase.
  • Another suitable method for the preparation of a soap rich phase may involve casting or extrusion of a soap rich composition.
  • the smooth (preferably non-soap surfactant) phase may also be prepared e.g. by extrusion, casting or other shaping methods.
  • Seperately prepared soap rich phase and non-soap surfactant rich phase can then be adhered to other parts of the tablet for example by gentle pressing or by usage of an adhesive material.
  • a seperately prepared solid phase e.g. of compressed particulate meterials can be combined with one ore more pre-prepared soap rich phases e.g. by gentle co-compression.
  • a tablet of this invention may be intended for use in machine dishwashing. Such tablets will typically contain salts, such as over 60 wt% of the tablet.
  • Water soluble salts typically used in machine dishwashing compositions are phosphates (including condensed phosphates) carbonates and silicates, generally as alkali metal salts.
  • Water soluble alkali metal salts selected from phosphates, carbonates and silicates may provide 60 wt% or more of a dishwashing composition.
  • a tablet of this invention will be intended for fabric washing.
  • the tablet will be likely to contain at least 2 wt%, probably at least 5 wt%, up to 40 or 50 wt% soap surfactant based on the whole tablet, and from 5 to 80 wt% detergency builder, based on the whole tablet.
  • compositions which are used in tablets of the invention will contain one or more detergent surfactants.
  • these preferably provide from 5 to 50% by weight of the overall tablet composition, more preferably from 8 or 9% by weight of the overall composition up to 40% or 50% by weight.
  • Surfactant may be anionic (soap or soap), cationic, zwitterionic, amphoteric, nonionic or a combination of these.
  • Anionic surfactant may be present in an amount from 0.5 to 50% by weight, preferably from 2% or 4% up to 30% or 40% by weight of the tablet composition.
  • Synthetic (i.e. non-soap) anionic surfactants are well known to those skilled in the art.
  • alkylbenzene sulphonates particularly sodium linear alkylbenzene sulphonates having an alkyl chain length of C 8 -C 15 ; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
  • Primary alkyl sulphate having the formula ROSO 3 - M + in which R is an alkyl or alkenyl chain of 8 to 18 carbon atoms especially 10 to 14 carbon atoms and M + is a solubilising cation, is commercially significant as an anionic surfactant.
  • Linear alkyl benzene sulphonate of the formula where R is linear alkyl of 8 to 15 carbon atoms and M + is a solubilising cation, especially sodium, is also a commercially significant anionic surfactant.
  • such linear alkyl benzene sulphonate or primary alkyl sulphate of the formula above, or a mixture thereof will be the desired anionic surfactant and may provide 75 to 100 wt% of any anionic soap surfactant in the composition.
  • the amount of non-soap anionic surfactant lies in a range from 5 to 20 wt% of the tablet composition.
  • Soaps for use in accordance to the invention are preferably alkali metal or alkaline earth metal salts of naturally occuring fatty acids, preferably sodium soaps derived from naturally occurring fatty acids, for example, the fatty acids from coconut oil, beef tallow, sunflower or hardened rapeseed oil.
  • soaps are selected from C 10 to C 20 soaps for example from C 16 to C 18 or C 12 soaps.
  • Suitable nonionic surfactant compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide.
  • Nonionic surfactant compounds are alkyl (C 8-22 ) phenol-ethylene oxide condensates, the condensation products of linear or branched aliphatic C 8-20 primary or secondary alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylene-diamine.
  • the primary and secondary alcohol ethoxylates especially the C 9-11 and C 12-15 primary and secondary alcohols ethoxylated with an average of from 5 to 20 moles of ethylene oxide per mole of alcohol.
  • the amount of nonionic surfactant lies in a range from 4 to 40%, better 4 or 5 to 30% by weight of the whole tablet.
  • nonionic surfactants are liquids. These may be absorbed onto particles of the composition.
  • the surfactant may be wholy nonionic, in an amount below 5 wt% of the whole tablet although it is known to include some anionic surfactant and to use up to 10 wt% surfactant in total.
  • a composition which is used in tablets of the invention will usually contain from 5 to 80%, more usually 15 to 60% by weight of detergency builder. This may be provided wholly by water soluble materials, or may be provided in large part or even entirely by water-insoluble material with water-softening properties. Water-insoluble detergency builder may be present as 5 to 80 wt%, better 5 to 60 wt% of the composition.
  • Alkali metal aluminosilicates are strongly favoured as environmentally acceptable water-insoluble builders for fabric washing.
  • Alkali metal (preferably sodium) aluminosilicates may be either crystalline or amorphous or mixtures thereof, having the general formula: 0.8 - 1.5 Na 2 O.Al 2 O 3 . 0.8 - 6 SiO 2 . xH 2 O
  • xH2O xH2O
  • xH2O calcium ion exchange capacity
  • the preferred sodium aluminosilicates contain 1.5-3.5 SiO 2 units (in the formula above). Both the amorphous and the crystalline materials can be prepared readily by reaction between sodium silicate and sodium aluminate, as amply described in the literature.
  • Suitable crystalline sodium aluminosilicate ion-exchange detergency builders are described, for example, in GB 1429143 (Procter & Gamble).
  • the preferred sodium aluminosilicates of this type are the well known commercially available zeolites A and X, the novel zeolite P described and claimed in EP 384070 (Unilever) and mixtures thereof.
  • a water-insoluble detergency builder could be a layered sodium silicate as described in US 4664839.
  • NaSKS-6 is the trademark for a crystalline layered silicate marketed by Hoechst (commonly abbreviated as "SKS-6").
  • KSKS-6 has the delta-Na 2 SiO 5 morphology form of layered silicate. It can be prepared by methods such as described in DE-A-3,417,649 and DE-A-3,742,043.
  • layered silicates such as those having the general formula NaMSi x O 2x+1 ⁇ yH 2 O wherein M is sodium or hydrogen, x is a number from 1.9 to 4, preferably 2, and y is a number from 0 to 20, preferably 0 can be used.
  • Water-soluble phosphorous-containing inorganic detergency builders include the alkali-metal orthophosphates, metaphosphates, pyrophosphates and polyphosphates.
  • Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
  • Non-phosphorous water-soluble builders may be organic or inorganic.
  • Inorganic builders that may be present include alkali metal (generally sodium) carbonate; while organic builders include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono- di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates and hydroxyethyliminodiacetates.
  • alkali metal generally sodium
  • organic builders include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono- di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dip
  • At least one region (preferably the second region) of a fabric washing tablet preferably include polycarboxylate polymers, more especially polyacrylates and acrylic/maleic copolymers which can function as builders and also inhibit unwanted deposition onto fabric from the wash liquor.
  • Tablets according to the invention may contain a bleach system in at least one region of a tablet, preferably in the second region.
  • This preferably comprises one or more peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which may be employed in conjunction with activators to improve bleaching action at low wash temperatures. If any peroxygen compound is present, the amount is likely to lie in a range from 10 to 25% by weight of the composition.
  • Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and sodium percarbonate, advantageously employed together with an activator.
  • Bleach activators also referred to as bleach precursors
  • Preferred examples include peracetic acid precursors, for example, tetraacetylethylene diamine (TAED), now in widespread commercial use in conjunction with sodium perborate; and perbenzoic acid precursors.
  • TAED tetraacetylethylene diamine
  • perbenzoic acid precursors perbenzoic acid precursors.
  • the quaternary ammonium and phosphonium bleach activators disclosed in US 4751015 and US 4818426 are also of interest.
  • bleach activator which may be used, but which is not a bleach precursor, is a transition metal catalyst as disclosed in EP-A-458397, EP-A-458398 and EP-A-549272.
  • a bleach system may also include a bleach stabiliser (heavy metal sequestrant) such as ethylenediamine tetramethylene phosphonate and diethylenetriamine pentamethylene phosphonate.
  • a bleach is present and is a water-soluble inorganic peroxygen bleach, the amount may well be from 10% to 25% by weight of the composition.
  • the detergent tablets of the invention may also contain (preferably in the second region) one of the detergency enzymes well known in the art for their ability to degrade and aid in the removal of various soils and stains.
  • Suitable enzymes include the various proteases, cellulases, lipases, amylases, and mixtures thereof, which are designed to remove a variety of soils and stains from fabrics.
  • suitable proteases are Maxatase (Trade Mark), as supplied by Gist-Brocades N.V., Delft, Holland, and Alcalase (Trade Mark), and Savinase (Trade Mark), as supplied by Novo Industri A/S, Copenhagen, Denmark.
  • Detergency enzymes are commonly employed in the form of granules or marumes, optionally with a protective coating, in amount of from about 0.1% to about 3.0% by weight of the composition; and these granules or marumes present no problems with respect to compaction to form a tablet.
  • the detergent tablets of the invention may also contain (preferably in the second region) a fluorescer (optical brightener), for example, Tinopal (Trade Mark) DMS or Tinopal CBS available from Ciba-Geigy AG, Basel, Switzerland.
  • a fluorescer optical brightener
  • Tinopal DMS is disodium 4,4'bis-(2-morpholino-4-anilino-s-triazin-6-ylamino) stilbene disulphonate
  • Tinopal CBS is disodium 2,2'-bis-(phenyl-styryl) disulphonate.
  • An antifoam material is advantageously included (preferably in the second region), especially if a detergent tablet is primarily intended for use in front-loading drum-type automatic washing machines.
  • Suitable antifoam materials are usually in granular form, such as those described in EP 266863A (Unilever).
  • Such antifoam granules typically comprise a mixture of silicone oil, petroleum jelly, hydrophobic silica and alkyl phosphate as antifoam active material, absorbed onto a porous absorbed water-soluble carbonate-based inorganic carrier material.
  • Antifoam granules may be present in an amount up to 5% by weight of the composition.
  • a detergent tablet of the invention includes an amount of an alkali metal silicate, particularly sodium ortho-, meta- or disilicate.
  • an alkali metal silicate particularly sodium ortho-, meta- or disilicate.
  • the presence of such alkali metal silicates at levels, for example, of 0.1 to 10 wt%, may be advantageous in providing protection against the corrosion of metal parts in washing machines, besides providing some measure of building and giving processing benefits in manufacture of the particulate material which is compacted into tablets.
  • a tablet for fabric washing will generally not contain more than 15 wt% silicate.
  • a tablet for machine dishwashing will often contain more than 20 wt% silicate.
  • the silicate is present in the second region of the tablet.
  • compositions which can optionally be employed in a region of a fabric washing detergent of the invention tablet include antiredeposition agents such as sodium carboxymethylcellulose, straight-chain polyvinyl pyrrolidone and the cellulose ethers such as methyl cellulose and ethyl hydroxyethyl cellulose, fabric-softening agents; heavy metal sequestrants such as EDTA; perfumes; and colorants or coloured speckles.
  • antiredeposition agents such as sodium carboxymethylcellulose, straight-chain polyvinyl pyrrolidone and the cellulose ethers such as methyl cellulose and ethyl hydroxyethyl cellulose, fabric-softening agents
  • heavy metal sequestrants such as EDTA
  • perfumes and colorants or coloured speckles.
  • dispersing aids are water-swellable polymers (e.g. SCMC) highly soluble materials (e.g. sodium citrate, potassium carbonate or sodium acetate) or sodium tripolyphospate with preferably at least 40% of the anhydrous phase I form.
  • SCMC water-swellable polymers
  • highly soluble materials e.g. sodium citrate, potassium carbonate or sodium acetate
  • sodium tripolyphospate preferably at least 40% of the anhydrous phase I form.
  • the first soap rich region of the cleaning tablet may advantageoulsy be prepared by compacting particles with a high soap content as described above. Preferably these particles have a mean particle size of from 100 to 1000 ⁇ m.
  • the second region of a detergent tablet of this invention is a preferably a matrix of compacted particles.
  • the particulate composition has a mean particle size in the range from 200 to 2000 ⁇ m, more preferably from 250 to 1400 ⁇ m. Fine particles, smaller than 180 ⁇ m or 200 ⁇ m may be eliminated by sieving before tableting, if desired, although we have observed that this is not always essential.
  • the starting particulate composition may in principle have any bulk density
  • the present invention is especially relevant to tablets made by compacting powders of relatively high bulk density, because of their greater tendency to exhibit disintegration and dispersion problems.
  • Such tablets have the advantage that, as compared with a tablet derived from a low bulk density powder, a given dose of composition can be presented as a smaller tablet.
  • the starting particulate composition may suitably have a bulk density of at least 400 g/litre, preferably at least 500 g/litre, and perhaps at least 600 g/litre.
  • Tableting machinery able to carry out the manufacture of tablets of the invention is known, for example suitable tablet presses are available from Fette and from Korch.
  • Tableting may be carried out at ambient temperature or at a temperature above ambient which may allow adequate strength to be achieved with less applied pressure during compaction.
  • the particulate composition is preferably supplied to the tableting machinery at an elevated temperature. This will of course supply heat to the tableting machinery, but the machinery may be heated in some other way also.
  • the size of a tablet will suitably range from 10 to 160 grams, preferably from 15 to 60 g, depending on the conditions of intended use, and whether it represents a dose for an average load in a fabric washing or dishwashing machine or a fractional part of such a dose.
  • the tablets may be of any shape. However, for ease of packaging they are preferably blocks of substantially uniform cross-section, such as cylinders or cuboids.
  • the overall density of a tablet preferably lies in a range from 1040 or 1050gm/litre up to 1600gm/litre.
  • a first particulate composition was prepared as follows. A powder was made of the following composition by pre-granulating the granule ingredients, followed by post-dosing the rest of the ingredients. Ingredient Parts by weight granules Linear alkylbenzene sulphonate, sodium salt 4.2 Alcohol ethoxylate nonionic, avg. 7EO 1.8 C16-18 soap 0.3 Zeolite A24 9.3 Sodium acetate, 3aq.
  • Non-soap surfactant rich smooth phase preparation isoap surfactant rich smooth phase preparation
  • This smooth phase was prepared of the following composition: Ingredient Parts by weight Na-las 39.1 Nonionic 7EO 33.5 C12 soap 7.3 Monopropyleenglycol to 100
  • the mixture was heated to 80°C and casted into moulds and cooled to 20°C to form firm, 5 grammes smooth, semi-solid parts of 45mm diameter.
  • a smooth part is then applied to the top of the tablet e.g. by gentle compression.
  • the resulting tablet is a three-layer tablet whereby the soap-rich layer is located between the solid phase and the smooth phase.
  • the compressed particulate phase had the following composition: Composition (%wt) P1 Na-LAS 4.15 Nonionic 7EO 1.82 Soap 0.33 zeolite A24 (anhydrous) 9.30 Na Acetate.3aq 1.18 Na Carbonate 1.38 SCMC (68%) 0.18 Moisture, salts, NDOM 1.67 Antifoam granule 1.01 Fluorescer granule (15 % active) 2.31 STP HPA 48.1 Nabion/Disilicate co granule. 2.50 TAED (as gran.83%) 4.52 Coated Percarbonate 17.2 Dequest 2047 (43%) 2.70 Enzymes 0.94 Perfume 0.71 TOTAL 100.0
  • compositions were used for the intermediate phase: Composition (%wt) I1 I2 Soap granules (Prisavon 1878 ex Uniqema) 25 50 Granular sodium sulphate 75 50
  • the semi-solid phase had the following composition: Composition (%wt) S1 Na-LAS 32.90 Nonionic 5EO 27.35 Na soap (C16/C18) 2.96 Tween 40 12.05 DiPropyleneGlycol 17.77 Dye 0.011 Water 6.96 Total 100
  • Example 2 a tablet consisting of a compressed particulate phase, an intermediate phase and a semi-solid phase was produced by first compressing 25 gr of composition P1 in a Fette tabletting machine. An intermediate phase was then formed on top of this particulate phase, by compressing 2 gr of composition I1 in the same Fette tabletting machine.
  • the semi-solid phase was produced by casting 5 gr of liquid composition S1 at 90°C into a mould, after which the phase was let to solidify. The semi-solid phase was then glued onto the intermediate phase with 0.3 gr of a hot melt water-soluble glue, to form the complete tablet.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP20040077426 2003-10-10 2004-08-31 Compositions détergentes Expired - Lifetime EP1522575B1 (fr)

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EP20040077426 EP1522575B1 (fr) 2003-10-10 2004-08-31 Compositions détergentes

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EP03256401 2003-10-10
EP03256401 2003-10-10
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EP04251448 2004-03-12
EP20040077426 EP1522575B1 (fr) 2003-10-10 2004-08-31 Compositions détergentes

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1746151A1 (fr) * 2005-07-20 2007-01-24 Unilever N.V. Pastilles de composition détergente

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999041353A1 (fr) * 1998-02-10 1999-08-19 Unilever Plc Compositions detergentes en pastilles
WO2001029162A1 (fr) * 1999-10-21 2001-04-26 Henkel Kommanditgesellschaft Auf Aktien Corps moules detergents et nettoyants presentant une resistance amelioree a l'abrasion

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999041353A1 (fr) * 1998-02-10 1999-08-19 Unilever Plc Compositions detergentes en pastilles
WO2001029162A1 (fr) * 1999-10-21 2001-04-26 Henkel Kommanditgesellschaft Auf Aktien Corps moules detergents et nettoyants presentant une resistance amelioree a l'abrasion

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1746151A1 (fr) * 2005-07-20 2007-01-24 Unilever N.V. Pastilles de composition détergente

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